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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items DB07268 - ≥98% , CAS No.929007-72-7
Synonyms
MFCD26960941 | 2-((2-(3-Hydroxyanilino)pyrimidin-4-yl)amino)benzamide | EX-A2356 | NCGC00378943-01 | AS-56032 | 4-anilinopyrimidine 2b | N11417 | BDBM15978 | HY-15737 | 2-((2-((3-Hydroxyphenyl)amino)pyrimidin-4-yl)amino)benzamide | 2-[[2-(3-hydroxyanilino
Shipped In
Hielera + almohadillas de hielo
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a -20°C Ships Hielera + almohadillas de hielo Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general El DB07268 es un inhibidor potente y selectivo de JNK1 con un valor IC50 de 9 nM.
Specifications Sinónimos
MFCD26960941 | 2-((2-(3-Hydroxyanilino)pyrimidin-4-yl)amino)benzamide | EX-A2356 | NCGC00378943-01 | AS-56032 | 4-anilinopyrimidine 2b | N11417 | BDBM15978 | HY-15737 | 2-((2-((3-Hydroxyphenyl)amino)pyrimidin-4-yl)amino)benzamide | 2-[[2-(3-hydroxyanilino
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Este compuesto presenta cierto grado de selectividad frente a bastantes quinasas, con las excepciones de CHK1, CK2 y PLK. Aunque el compuesto 2b(DB-07268) muestra una potencia submicromolar frente a estas tres quinasas, parece exhibir al menos entre 70 y
Condiciones de almacenamiento de almacenamiento
Conservar a -20°C
Enviado en
Hielera + almohadillas de hielo
Nombres e identificadores Sonrisas canónicas C1=CC=C(C(=C1)C(=O)N)NC2=NC(=NC=C2)NC3=CC(=CC=C3)O IUPAC Name 2-[[2-(3-hydroxyanilino)pyrimidin-4-yl]amino]benzamide InChIKey QHPKKGUGRGRSGA-UHFFFAOYSA-N INCHI 1S/C17H15N5O2/c18-16(24)13-6-1-2-7-14(13)21-15-8-9-19-17(22-15)20-11-4-3-5-12(23)10-11/h1-10,23H,(H2,18,24)(H2,19,20,21,22) Isómeros SMILES C1=CC=C(C(=C1)C(=O)N)NC2=NC(=NC=C2)NC3=CC(=CC=C3)O Peso molecular 321.33 Reaxy-Rn 10700980 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10700980&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Benzamides Alternative Parents m-Aminophenols Benzoyl derivatives Aniline and substituted anilines 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Aminopyrimidines and derivatives Imidolactams Vinylogous amides Heteroaromatic compounds Primary carboxylic acid amides Amino acids and derivatives Secondary amines Azacyclic compounds Hydrocarbon derivatives Organic oxides Organooxygen compounds Organopnictogen compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Benzamide - M-aminophenol - Aminophenol - Benzoyl - Aniline or substituted anilines - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aminopyrimidine - Phenol - Imidolactam - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Carboxamide group - Primary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Secondary amine - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached to a benzene ring. External Descriptors aminopyrimidine - benzamides Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad 25°C: DMSO Peso molecular 321.330 g/mol XLogP3 3.000 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 5 Exact Mass 321.123 Da Monoisotopic Mass 321.123 Da Topological Polar Surface Area 113.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 422.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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